BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

132 related articles for article (PubMed ID: 15006694)

  • 1. Pleiotropic and diverse expression of ZFHX1B gene transcripts during mouse and human development supports the various clinical manifestations of the "Mowat-Wilson" syndrome.
    Bassez G; Camand OJ; Cacheux V; Kobetz A; Dastot-Le Moal F; Marchant D; Catala M; Abitbol M; Goossens M
    Neurobiol Dis; 2004 Mar; 15(2):240-50. PubMed ID: 15006694
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Neural crest-specific removal of Zfhx1b in mouse leads to a wide range of neurocristopathies reminiscent of Mowat-Wilson syndrome.
    Van de Putte T; Francis A; Nelles L; van Grunsven LA; Huylebroeck D
    Hum Mol Genet; 2007 Jun; 16(12):1423-36. PubMed ID: 17478475
    [TBL] [Abstract][Full Text] [Related]  

  • 3. ZFHX1B mutations in patients with Mowat-Wilson syndrome.
    Dastot-Le Moal F; Wilson M; Mowat D; Collot N; Niel F; Goossens M
    Hum Mutat; 2007 Apr; 28(4):313-21. PubMed ID: 17203459
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Genetic interaction between Sox10 and Zfhx1b during enteric nervous system development.
    Stanchina L; Van de Putte T; Goossens M; Huylebroeck D; Bondurand N
    Dev Biol; 2010 May; 341(2):416-28. PubMed ID: 20206619
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Clinical and mutational spectrum of Mowat-Wilson syndrome.
    Zweier C; Thiel CT; Dufke A; Crow YJ; Meinecke P; Suri M; Ala-Mello S; Beemer F; Bernasconi S; Bianchi P; Bier A; Devriendt K; Dimitrov B; Firth H; Gallagher RC; Garavelli L; Gillessen-Kaesbach G; Hudgins L; Kääriäinen H; Karstens S; Krantz I; Mannhardt A; Medne L; Mücke J; Kibaek M; Krogh LN; Peippo M; Rittinger O; Schulz S; Schelley SL; Temple IK; Dennis NR; Van der Knaap MS; Wheeler P; Yerushalmi B; Zenker M; Seidel H; Lachmeijer A; Prescott T; Kraus C; Lowry RB; Rauch A
    Eur J Med Genet; 2005; 48(2):97-111. PubMed ID: 16053902
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Nonsense mutations of the ZFHX1B gene in two Japanese girls with Mowat-Wilson syndrome.
    Sasongko TH; Sadewa AH; Gunadi ; Lee MJ; Koterazawa K; Nishio H
    Kobe J Med Sci; 2007; 53(4):157-62. PubMed ID: 17932455
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Intrahepatic biliary anomalies in a patient with Mowat-Wilson syndrome uncover a role for the zinc finger homeobox gene zfhx1b in vertebrate biliary development.
    Cui S; Erlichman J; Russo P; Haber BA; Matthews RP
    J Pediatr Gastroenterol Nutr; 2011 Mar; 52(3):339-44. PubMed ID: 21336163
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Mowat-Wilson syndrome affecting 3 siblings.
    Ohtsuka M; Oguni H; Ito Y; Nakayama T; Matsuo M; Osawa M; Saito K; Yamada Y; Wakamatsu N
    J Child Neurol; 2008 Mar; 23(3):274-8. PubMed ID: 18230842
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Atypical Mowat-Wilson patient confirms the importance of the novel association between ZFHX1B/SIP1 and NuRD corepressor complex.
    Verstappen G; van Grunsven LA; Michiels C; Van de Putte T; Souopgui J; Van Damme J; Bellefroid E; Vandekerckhove J; Huylebroeck D
    Hum Mol Genet; 2008 Apr; 17(8):1175-83. PubMed ID: 18182442
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Mowat-Wilson syndrome: an underdiagnosed syndrome?
    Engenheiro E; Møller RS; Pinto M; Soares G; Nikanorova M; Carreira IM; Ullmann R; Tommerup N; Tümer Z
    Clin Genet; 2008 Jun; 73(6):579-84. PubMed ID: 18445050
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Mouse Zic5 deficiency results in neural tube defects and hypoplasia of cephalic neural crest derivatives.
    Inoue T; Hatayama M; Tohmonda T; Itohara S; Aruga J; Mikoshiba K
    Dev Biol; 2004 Jun; 270(1):146-62. PubMed ID: 15136147
    [TBL] [Abstract][Full Text] [Related]  

  • 12. SATB2 is a multifunctional determinant of craniofacial patterning and osteoblast differentiation.
    Dobreva G; Chahrour M; Dautzenberg M; Chirivella L; Kanzler B; Fariñas I; Karsenty G; Grosschedl R
    Cell; 2006 Jun; 125(5):971-86. PubMed ID: 16751105
    [TBL] [Abstract][Full Text] [Related]  

  • 13. miR-200b mediates post-transcriptional repression of ZFHX1B.
    Christoffersen NR; Silahtaroglu A; Orom UA; Kauppinen S; Lund AH
    RNA; 2007 Aug; 13(8):1172-8. PubMed ID: 17585049
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Atrophin 2 recruits histone deacetylase and is required for the function of multiple signaling centers during mouse embryogenesis.
    Zoltewicz JS; Stewart NJ; Leung R; Peterson AS
    Development; 2004 Jan; 131(1):3-14. PubMed ID: 14645126
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Frameshift mutation of the zinc finger homeo box 1 B gene in syndromic corpus callosum agenesis (Mowat-Wilson syndrome).
    Sztriha L; Espinosa-Parrilla Y; Gururaj A; Amiel J; Lyonnet S; Gerami S; Johansen JG
    Neuropediatrics; 2003 Dec; 34(6):322-5. PubMed ID: 14681759
    [TBL] [Abstract][Full Text] [Related]  

  • 16. "Mowat-Wilson" syndrome with and without Hirschsprung disease is a distinct, recognizable multiple congenital anomalies-mental retardation syndrome caused by mutations in the zinc finger homeo box 1B gene.
    Zweier C; Albrecht B; Mitulla B; Behrens R; Beese M; Gillessen-Kaesbach G; Rott HD; Rauch A
    Am J Med Genet; 2002 Mar; 108(3):177-81. PubMed ID: 11891681
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Alternative usage of Otx2 promoters during mouse development.
    Fossat N; Courtois V; Chatelain G; Brun G; Lamonerie T
    Dev Dyn; 2005 May; 233(1):154-60. PubMed ID: 15759271
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Cardiac malformations, adrenal agenesis, neural crest defects and exencephaly in mice lacking Cited2, a new Tfap2 co-activator.
    Bamforth SD; Bragança J; Eloranta JJ; Murdoch JN; Marques FI; Kranc KR; Farza H; Henderson DJ; Hurst HC; Bhattacharya S
    Nat Genet; 2001 Dec; 29(4):469-74. PubMed ID: 11694877
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Role of the vascular endothelial growth factor isoforms in retinal angiogenesis and DiGeorge syndrome.
    Stalmans I
    Verh K Acad Geneeskd Belg; 2005; 67(4):229-76. PubMed ID: 16334858
    [TBL] [Abstract][Full Text] [Related]  

  • 20. TGIF, a gene associated with human brain defects, regulates neuronal development.
    Knepper JL; James AC; Ming JE
    Dev Dyn; 2006 Jun; 235(6):1482-90. PubMed ID: 16534781
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.